Product Details

SNP ID
rs587780369
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.20:63406650 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCACTGGCCCAGCGCCGCCTCACTT[C/A]CTGGGCCCGGCCCAGCCCACGTCAC
Phenotype
MIM: 602235
Polymorphism
C/A, Transversion substitution
Allele Nomenclature
Literature Links
KCNQ2 PubMed Links

Gene Details

Gene
KCNQ2
Gene Name
potassium voltage-gated channel subfamily Q member 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_004518.5 2233 Missense Mutation AGG,AGT R843S NP_004509.2
NM_172106.2 2233 Missense Mutation AGG,AGT R853S NP_742104.1
NM_172107.3 2233 Missense Mutation AGG,AGT R871S NP_742105.1
NM_172108.4 2233 Missense Mutation AGG,AGT R840S NP_742106.1
NM_172109.2 2233 Intron NP_742107.1
XM_011528810.1 2233 Missense Mutation AGG,AGT R889S XP_011527112.1
XM_011528811.1 2233 Missense Mutation AGG,AGT R879S XP_011527113.1
XM_017027841.1 2233 Missense Mutation AGG,AGT R888S XP_016883330.1
XM_017027842.1 2233 Missense Mutation AGG,AGT R867S XP_016883331.1
XM_017027843.1 2233 Missense Mutation AGG,AGT R866S XP_016883332.1
XM_017027844.1 2233 Missense Mutation AGG,AGT R852S XP_016883333.1
XM_017027845.1 2233 Missense Mutation AGG,AGT R543S XP_016883334.1
Gene
LOC100130152
Gene Name
uncharacterized LOC100130152
There are no transcripts associated with this gene.

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